Effects of pathophysiological concentrations of albumin on NHE3 activity and cell proliferation in primary cultures of human proximal tubule cells

被引:29
作者
Lee, EM
Pollock, CA
Drumm, K
Barden, JA
Poronnik, P [1 ]
机构
[1] Univ Queensland, Sch Biomed Sci, St Lucia, Qld 4072, Australia
[2] Univ Sydney, Royal N Shore Hosp, Kolling Inst Med Res, Dept Med,Renal Res Grp, St Leonards, NSW 2065, Australia
[3] Univ Sydney, Dept Anat & Histol, Sydney, NSW 2006, Australia
[4] Univ Wurzburg, Inst Physiol, D-97070 Wurzburg, Germany
关键词
proteinuria; sodium-hydrogen exchange; sodium retention;
D O I
10.1152/ajprenal.00442.2002
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The progression of renal disease correlates strongly with hypertension and the degree of proteinuria, suggesting a link between excessive Na+ reabsorption and exposure of the proximal tubule to protein. The present study investigated the effects of albumin on cell growth and Na+ uptake in primary cultures of human proximal tubule cells (PTC). Albumin (1.0 mg/ml) increased cell proliferation to 134.1 +/- 11.8% (P < 0.001) of control levels with no change in levels of apoptosis. Exposure to 0.1 and 1.0 mg/ml albumin increased total Na-22(+) uptake to 119.1 +/- 6.3% (P = 0.005) and 115.6 +/- 5.3% (P < 0.006) of control levels, respectively, because of an increase in Na+/H+ exchanger isoform 3 (NHE3) activity. This was associated with an increase in NHE3 mRNA to 161.1 +/- 15.1% (P < 0.005) of control levels in response to 0.1 mg/ml albumin. Using confocal microscopy with a novel antibody raised against the predicted extracellular NH2 terminus of human NHE3, we observed in nonpermeabilized cells that exposure of PTC to albumin (0.1 and 1.0 mg/ml) increased NHE3 at the cell surface to 115.4 +/- 2.7% (P < 0.0005) and 122.4 +/- 3.7% (P < 0.0001) of control levels, respectively. This effect was paralleled by significant increases in NHE3 in the subplasmalemmal region as measured in permeabilized cells. These albumin-induced increases in expression and activity of NHE3 in PTC suggest a possible mechanism for Na+ retention in response to proteinuria.
引用
收藏
页码:F748 / F757
页数:10
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